Clearance Summary
STANBIO DIRECT URIC ACID TEST SET #0770 received FDA 510(k) clearance under submission number K800190, sponsored by Stanbio Laboratory. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1980-02-13.
- Submission: K800190
- Applicant / Sponsor: Stanbio Laboratory
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1775
- Decision date: 1980-02-13
Classification & Regulation
This clearance is catalogued under FDA product code CDH and 21 CFR 862.1775, within the Clinical Chemistry review panel as a Class I device.